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FDA 510(k)

LATERAL BUTTON

K-Number: K112296 · 2011-12-01

ApplicantT.A.G. Medical Products Corporation, Ltd.
Decision Date2011-12-01
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LATERAL BUTTON is the device name listed in this FDA 510(k) record. The listed applicant is T.A.G. Medical Products Corporation, Ltd.. It received FDA 510(k) clearance on 2011-12-01 under 510(k) number K112296. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LATERAL BUTTON?

LATERAL BUTTON is a medical device that received FDA 510(k) clearance on 2011-12-01. The listed applicant is T.A.G. Medical Products Corporation, Ltd.. The 510(k) number is K112296.

When did LATERAL BUTTON receive FDA 510(k) clearance?

LATERAL BUTTON received FDA 510(k) clearance on 2011-12-01, under 510(k) number K112296.

Who is the listed applicant for LATERAL BUTTON?

The FDA 510(k) record lists T.A.G. Medical Products Corporation, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LATERAL BUTTON?

The FDA product code for LATERAL BUTTON is MBI.

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Related Devices (Code: MBI)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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